A method for manufacturing composite materials from a parent substance containing silicon nitride and metal silicide, having fixed electrical properties. The molded articles are made, virtually with their final contours, prior to a sintering operation. The parent substance containing Si3N4 and a metal silicide is subjected to a gas pressure sintering in a nitrogenous atmosphere. The metal silicide is of the form Me5Si3, where Me is a metal. As a function of a sintering temperature, a lower limit of partial nitrogen pressures is selected so that Si3N4 is stable at the lower limit and an upper limit of the partial nitrogen pressures is selected so that Me5Si3 is stable at the upper limit. The resulting composite material is a silicon-containing composite material made of Si3N4 and the metal silicide. The metal silicide is selected from the group of Nb5Si3, V5Si3, Ta5Si3 and W5Si3.
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20. A silicon-containing composite material comprising a silicon-containing material made of Si3N4 and a metal silicide, wherein the metal silicide is selected from the group of Nb5Si3, V5S3, TaSi3 and W5Si3, wherein the metal silicide contains carbon.
1. A method for fabricating a composite material, the method comprising the steps of:
providing a parent substance containing a silicon nitride and a metal silicide, the silicon nitride being Si3N4 and the metal silicide being of a form Me5Si3, where Me is a metal; establishing, as a function of a sintering temperature, an upper limit and a lower limit of partial nitrogen pressures so that the silicon nitride is stable at the lower limit and the metal silicide is stable at the upper limit; and gas pressure sintering the parent substance in a nitrogenous atmosphere based on the lower limit and the upper limit.
2. The method of
3. The method of
4. The method of
6. The method of
7. The method of
10. The method of
(a) forming the parent substance into a desired shape by one of ceramic injection molding and cold-isostatic pressing before the step of gas pressure sintering; and (b) (i) forming the parent substance into the desired shape by the one of the ceramic injection molding and the cold-isostatic pressing before the step of gas pressure sintering, and (ii) forming the composite material by green processing subsequent to the step of gas pressure sintering. 11. The method of
12. The method of
13. The method of
14. The method of
15. The method of
16. The method of
17. The method of
the metal of the metal silicide is molybdenum; and the upper limit is set as an upper limit of partial N2 pressures (pN2) according to a first equation of y1=5.3071·ln(T)-37.014, and the lower limit is set as a lower limit of the partial N2 pressures (pN2) according to a second equation of y2=7.3494·ln(T)-54.124, where y1 and y2 represent lg(pN2 [bar]) values. 18. The method of
the metal of the metal silicide is niobium; and the upper limit is set as an upper limit of partial N2 pressures (pN2) according to a first equation of y1=7.8968·ln(T)-58.8, and the lower limit is set as a lower limit of the partial N2 pressures (pN2) according to a second equation of y2=8.2598·ln(T)-62.064, where y1 and y2 represent lg(pN2 [bar]) values. 19. The method of
21. The composite material of
22. The composite material of
24. The composite material of
25. The composite material of
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The present invention relates to a method for fabricating a composite material out of a parent substance containing silicon nitride and a metal silicide, through gas pressure sintering in a nitrogenous atmosphere and a silicon-containing composite material, whose silicon-containing constituents are made of Si3N4 and of a metal silicide.
There are composite materials, which contain silicon nitride and metal silicide, and methods for their preparation. The fabrication of such materials through single-axial not pressing (unconfined sintering under pressure) is discussed in German Published Patent Application Nos. 37 34 274 and 36 06 403, in which the parent substance contains Si3 N4 and the metal silicide MoSi2, and in European Patent Application No. 0 335 382, in which the parent substance contains Si3 N4 and MO5 Si3 as the metal silicide and carbon, and the fabricated material contains as metal silicide, Mo5Si3C or, more precisely, Mo5-XSi3C1-Y (0≦X≦2; 0≦Y≦1). The electrical properties of the materials fabricated in this manner are able to be selectively adjustable. It is believed that the method is industrial and requires considerable outlay for energy consumption and that the application of the method only permits fabrication of complex geometrical structures in expensive, hard-machining operations.
German Published Patent Application No. 195 00 832, i.e., European Patent Application No. 0 721 925, discusses the fabrication of highly heat-resistant silicon nitride composite materials, which contain a reinforcement component of Me5Si3 and, moreover, MeSi2 or MeSi2, and silicides of other stoichiometries, Me standing for metal. Mixed into the parent substance as metal silicide are MeSi2 and Me5Si3, or only MeSi2. The metals may be selected from the group including molybdenum, tungsten, chromium, tantalum, niobium, manganese and vanadium. The sintering is performed as gas pressure sintering (at N2 pressures of 100 bar), which makes it possible to fabricate molded articles (shaped bodies), virtually with their final contours, in ceramic injection molding or pressing processes, with subsequent green processing, or in hot-pressing (sintering under pressure) processes. Special electrical properties cannot be
An object of an exemplary embodiment of the present invention is an industrially simple and energy-saving method for fabricating composite materials containing silicon nitride and metal silicide and having fixed electrical properties, which makes it possible to manufacture the molded articles, virtually with their final contours, from the composite material, prior to the sintering operation, and to specify representatives of such composite materials in an exemplary method, where Me5 Si3 is introduced as the metal suicide into the parent substance, the partial pressure of the nitrogen being established as a function of the sintering temperature in such a way that, at the lower limit of the practical range, Si3N4 is still thermodynamically stable and, at the upper limit, Me5Si3, and is dissolved into a composite material of the type mentioned at the outset, the sit metal silicide being selected from the group Nb5Si3, V5Si3, Ta5Si3 and W5Si3.
To exploit the advantages of the gas-pressure sintering method, at the same time while manufacturing composite materials having fixed electrical properties it was ascertained that the electrical properties cannot be adjusted in a determinate fashion (definably) when N2 applied above a specific pressure range. During test trials, it was found that there is a range of the N 2 partial pressures within which one can prevent other silicon-containing components, besides Si3N4 and Me5Si3, from being present in the finished composite material. In this manner, composite materials were fabricated having fixed electrical properties. In comparison to the hot-pressing (sintering under pressure) method, the gas-pressure sintering method makes do with a much simpler sintering device. Compact, high-strength materials are able to be fabricated with the exemplary method to the present invention. In comparison to materials containing MeSi2, materials containing Me5Si3 are believed to a very low temperature dependency of the electrical conductivity.
The method is carried out in such a way that the metal silicide in the composite material has a carbon concentration (preferably between about 0.3 and about 0.6% by weight specific to the composite material), i.e., is present as Me5Si3(C).
The exemplary embodiments of the method according the present invention described in the following are believed to be particularly advantageous. However, they are merely provided by way of example, and suitable appropriate variations are possible, without departing from the scope of the claims.
To fabricate the composite materials, a preconditioned Si3N4 powder is first mixed with sinter additives, such as Al203, Y203, or the like, which (in terms of the entire inorganic concentration-, make up less than about 10% by weight, Me5Si3 in suitable percentages by weight and, in some instances, organic pressing and/or binding agents, with the addition of an organic solvent, which may be done in an attritor mill. The attrited suspension is dried, for example, in a rotary evaporator. From the dried powder, through cold-isostatic pressing at pressures of between about 150 and 250 MPa, molded articles are produced, which, subsequent to the pressing operation, can obtain their final shape in a green processing. Other processing possibilities following the introduction of appropriate binding agents, include ceramic injection molding (CIM) or extrusion. For debinding and/or presintening purposes, the molded articles are treated at approximately 600°C C. under a pressure of 1 bar in an inert gas atmosphere for about two hours, the organic constituents being removed, virtually without leaving any residues. The main sintering operation then follows, which may occur, for example, in a gas-pressure sintering furnace at a temperature within a range of about 1700 and 1900°C C., including between about 1800 and 1900°C C., under a defined partial N2 pressure (total pressure between about 0.1 MPa and 10 MPa), which is set so as to achieve thermodynamic equilibrium of the Si3N4 phase and the Me5Si3 or Me5Si3(C) phase during the sintering compression, i.e., to ensure they do not enter into any chemical reactions. The usable range of the partial N2 pressure at a specific temperature is dependent upon the metal silicide. In the diagrams of
respectively
and, for Nb-containing mixtures, the equations
respectively
y1 and y2 representing lg(pN2 [bar]) values. Below the limited range, Si3N4 reacts with Me5Si3. Above the limited range, Me5Si3 reacts with nitrogen. The curves were determined in serial investigations, in that, at a fixed temperature of between about 1700 and 1900°C C., the partial N2 pressures were determined at which Me5Si3 and Si3N4 are thermodynamically stable. The criterion that no reaction took place is, in each case, that only the desired silicon-containing phases are found in the X-ray diffractogram of the sintered material. The equations named above were then determined on the basis of these values, of known data, such as enthalpies of formation, and of thermodynamic functions. The sintering process takes about two to five hours.
The specific electrical resistance of the composite materials fabricated in accordance with the exemplary embodiment of the method of the present invention is adjusted through the selection of the metal in the silicide and the concentration and the distribution of the silicide in the composite material. Beyond the particular percolation range, specific electrical resistances of between about 1.7·10-4 Ωcm and 1·1012 Ωcm can be reproducibly adjusted with materials containing Nb5Si3(C), and of between about 1·10-5 Ωcm and 1·1012 Ωcm with materials containing Mo5Si3(C). The specific resistance is measured using the four-point method.
Using qualitative and quantitative chemical and physico-chemical analyses and radiographic phase analysis, one can verify that--apart from the carbon concentration and without consideration of the organic constituents--the sintered materials have the same composition as the mixture that the fabrication process originated with. During the sintering process in a graphite furnace, the carbon maybe contained in the metal silicide with a concentration, in terms of the composite material, of between about 0.3 and 0.6% by weight, and including with about 0.5% by weight. The room (ambient) temperature stabilities of the composite materials do not lie under 500 MPa.
Besides standing for niobium and molybdenum having comparable results for all metals of the 5th and 6th subgroup of the periodic table or system, Me can stand, in particular, for vanadium, tantalum, chromium and tungsten.
The exemplary embodiment of the method of the present invention is described in greater detail in the following on the basis of two special examples.
The parent substance was mixed from 36% by weight of Si3N4, 1.7% by weight of Al2O3, 2.38% by weight of Y2O3, 60 Nb5Si3% by weight and the usual pressing and/or binding agents. The average particle size of the Si3N4 was 0.7 μm, and that of the Nb,Si3 0.7 μm. The cold isostatic compression at 200 MPa was followed by a pre-sintering under an inert gas at up to 600°C C., argon being used (nitrogen also could have been used). Sintering subsequently took place at a partial N2 pressure of 0.5 MPa (total pressure 1 MPa) and 1800°C C. in a graphite furnace.
The density of the composite material obtained was 97% of the material density. The radiographic phase analysis performed after the sintering process yielded exclusively Si3N4 and Nb5Si3(C) as silicon-containing phases. As a specific electrical resistance, 3·6·10-3 Ωcm was determined at 25°C C. The temperature coefficient of the specific electrical resistance amounted to 2·10-4 K-1.
Besides the fact that the inorganic constituents of the parent substance were made up of 54% by weight of Si3N4, 2.6% by weight of Al2O3, 3.4% by weight of Y2O3, 40 Nb5Si3% by weight, the method was carried out in the same manner as in Example 1.
The analyses performed on the sintered material likewise yielded the attained material density amount of 97%, the radiographic phase analysis yielded exclusively Si3N4 and Nb5Si3(C) as silicon-containing phases, and 2·102 Ωcm at 25°C C. was determined as a specific electrical resistance.
Lindemann, Gert, Lindner, Friederike, Knoll, Guenter, Wiedmaier, Matthias
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| Aug 04 2000 | LINDNER, FRIEDERIKE | Robert Bosch GmbH | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 011252 | /0953 | |
| Aug 08 2000 | KNOLL, GUENTER | Robert Bosch GmbH | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 011252 | /0953 | |
| Oct 02 2000 | WIEDMAIER, MATTHIAS | Robert Bosch GmbH | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 011252 | /0953 | |
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